510(k) K100671

NOVABONE DENTAL PUTTY-BIOACTIVE SYNTHETIC BONE GRAFT by Novabone Products, LLC — Product Code LYC

K100671 is an FDA 510(k) premarket notification submitted by Novabone Products, LLC for the device "NOVABONE DENTAL PUTTY-BIOACTIVE SYNTHETIC BONE GRAFT". The FDA issued a decision of Substantially Equivalent on March 30, 2010. The device falls under product code LYC (Bone Grafting Material, Synthetic), a Class II device regulated under 21 CFR 872.3930. Novabone Products, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 30, 2010
Date Received
March 9, 2010
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bone Grafting Material, Synthetic
Device Class
Class II
Regulation Number
872.3930
Review Panel
DE
Submission Type

A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw.